1095281-91-6 Usage
General Description
6-chloro-7-methyl-2-trifluoromethyl-7H-purine is a chemical compound with a purine base structure. It contains a chloro group at the 6th position, a methyl group at the 7th position, and a trifluoromethyl group at the 2nd position of the purine ring. 6-chloro-7-methyl-2-trifluoromethyl-7H-purine has potential applications in the pharmaceutical industry, particularly in the development of novel drugs targeting purine receptors. It may also have biological activity as a purine analog, which could make it useful in medicinal chemistry research. Additionally, the presence of fluorine atoms can enhance the compound's properties, making it of interest for potential therapeutic use.
Check Digit Verification of cas no
The CAS Registry Mumber 1095281-91-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,5,2,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1095281-91:
(9*1)+(8*0)+(7*9)+(6*5)+(5*2)+(4*8)+(3*1)+(2*9)+(1*1)=166
166 % 10 = 6
So 1095281-91-6 is a valid CAS Registry Number.
1095281-91-6Relevant academic research and scientific papers
Synthetic studies directed towards agelasine analogs - Synthesis, tautomerism, and alkylation of 2-substituted N-methoxy-9-methyl-9H-purin-6- amines
Roggen, Heidi,Gundersen, Lise-Lotte
experimental part, p. 5099 - 5106 (2009/06/06)
N-Methoxy-9-methyl-9H-purin-6-amines, carrying various substituents in the 2 positions, were synthesized by the N-methylation of known 6-chloropurines, followed by a displacement of the chlorine. Great variations in the amino/imino tautomer ratio among the compounds studied were observed. The tautomers were identified by NMR methods. Treatment of N-methoxy-9-methyl-9H-purin-6-amines carrying alkyl, alkoxy, or amino substituents in the 2 position with benzyl bromide resulted in a mixture of N-7- and N6-benzylated compounds with the former as the major products. N-Methoxy-9-methyl-9H-purin-6-amines with strongly electronegative substituents at C-2 hardly reacted at all under the same set of reaction conditions. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
